Siemens Medical Solutions USA, Inc., Ultrasound DI is one of 13724 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Siemens Medical Solutions USA, Inc., Ultrasound DI - FDA 510(k) Clear...
Recent clearances: syngo. CT Single Source Dual Energy (twin beam), ACUSON SC2000 DIAGNOSTIC ULTRASOUND SYSTEM, ACUSON S2000 DIAGNOSTIC ULTRASOUND SYSTEM
11
Total
11
Cleared
0
Denied
Siemens Medical Solutions USA, Inc., Ultrasound DI has 11 FDA 510(k) cleared radiology devices. Based in Mountain View, US.
Historical record: 11 cleared submissions from 2007 to 2017.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Siemens Medical Solutions USA, Inc., Ultrasound DI
11 devices
Cleared
Feb 09, 2017
syngo. CT Single Source Dual Energy (twin beam)
Radiology
79d
Cleared
Dec 07, 2011
ACUSON SC2000 DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
40d
Cleared
Sep 16, 2011
ACUSON S2000 DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
9d
Cleared
Dec 22, 2008
SIEMENS ACUSON 2000 ULTRASOUND SYSTEM WITH ABVS TRANSDUCER
Radiology
244d
Cleared
Nov 13, 2008
ACUSON S2000 DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
106d
Cleared
Jun 04, 2008
MODIFICATION TO ACUSON X150 ULTRASOUND SYSTEM
Radiology
44d
Cleared
Apr 25, 2008
ACUSON X300 ULTRASOUND SYSTEM
Radiology
38d
Cleared
Oct 17, 2007
SEQUOIA PLUS DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
55d
Cleared
Sep 14, 2007
SIEMENS DIAGNOSTIC ULTRASOUND SYSTEMS
Radiology
46d
Cleared
May 16, 2007
MODIFICATION TO ACUSON X300 ULTRASOUND SYSTEM
Radiology
34d
Cleared
Jan 05, 2007
ACUSON ANTARES DIAGNOSTIC ULTRASOUND SYSTEM
Radiology
14d